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首页> 外文期刊>Supportive care in cancer: official journal of the Multinational Association of Supportive Care in Cancer >Prospective evaluation of the incidence of delayed nausea and vomiting in patients with colorectal cancer receiving oxaliplatin-based chemotherapy.
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Prospective evaluation of the incidence of delayed nausea and vomiting in patients with colorectal cancer receiving oxaliplatin-based chemotherapy.

机译:对接受以奥沙利铂为基础的化疗的结直肠癌患者延迟性恶心和呕吐发生率的前瞻性评估。

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This study sought to prospectively determine the frequency of delayed nausea and vomiting with oxaliplatin-based chemotherapy following day 1 prophylaxis with a 5-HT-(3) receptor antagonist and dexamethasone.Patients with colon cancer, ≥ age 18, with a performance status ≤ 2, receiving oxaliplatin (85-100 mg/m(2)) as part of a standard folinic acid, 5-fluorouracil, oxaliplatin regimen for the first time were eligible. All patients received a 5-HT(3) receptor antagonist and dexamethasone 20 mg on day 1 prior to oxaliplatin. No routine prophylaxis for delayed emesis was given. Antiemetic outcome was recorded in patient-completed diaries for the 120-h study period following oxaliplatin administration. Primary endpoint was frequency of delayed (24-120 h) emesis (vomiting/retching).Forty-one patients were enrolled and 39 are evaluable. Median age was 70 (34-85) and the female/male ratio was 20:19. Four patients (10%) experienced vomiting or retching during the delayed period. One patient vomited during the first 24 h after oxaliplatin. The overall (120 h) no emesis rate was 87% (34/39). Twenty-one patients (54%) developed delayed nausea. Nine patients had moderate or severe nausea. Eighteen patients (46%) took rescue antiemetics during the delayed period. Delayed and overall complete response (no emesis or use of rescue antiemetics) rates were 54% and 49%, respectively.The use of a 5-HT(3) antagonist and dexamethasone prior to oxaliplatin results in excellent control of nausea and vomiting (CR-90%) during the 24 h after chemotherapy. However, without further antiemetic treatment, complete response in the delayed period decreased to 54%. This study supports the need for routine antiemetic prophylaxis for delayed nausea and vomiting following oxaliplatin-based chemotherapy.
机译:这项研究旨在前瞻性确定使用5-HT-(3)受体拮抗剂和地塞米松预防的第1天后,以奥沙利铂为基础的化疗引起的延迟恶心和呕吐的频率。结肠癌患者,≥18岁,表现状态≤ 2,首次接受奥沙利铂(85-100 mg / m(2))作为标准亚叶酸,5-氟尿嘧啶和奥沙利铂方案的一部分。在奥沙利铂之前的第一天,所有患者均接受5-HT(3)受体拮抗剂和地塞米松20 mg。没有常规预防延迟呕吐的方法。在服用奥沙利铂后的120小时研究期间,患者完成的日记中记录了止吐结果。主要终点为延迟呕吐(呕吐/呕吐)(24-120小时)的频率。共有41例患者入组,其中39例可评估。中位年龄为70岁(34-85岁),男女比例为20:19。四名患者(10%)在延迟期内经历了呕吐或呕吐。一位患者在奥沙利铂治疗后的最初24小时内呕吐。总体(120小时)无呕吐率为87%(34/39)。 21名患者(54%)出现恶心延迟。 9名患者出现中度或重度恶心。 18名患者(46%)在延迟期间服用了止吐药。延迟和总体完全缓解率(无呕吐或使用催吐药)分别为54%和49%。在使用奥沙利铂之前使用5-HT(3)拮抗剂和地塞米松可以很好地控制恶心和呕吐(CR) -90%)在化疗后的24小时内。但是,如果不进行进一步的止吐治疗,则延迟期的完全缓解率降至54%。这项研究支持对基于奥沙利铂的化疗后延迟恶心和呕吐进行常规止吐的预防。

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